T14N (p.Thr14Asn) variant of CD19 (B-lymphocyte antigen CD19)
T14N (p.Thr14Asn) in CD19 (B-lymphocyte antigen CD19) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
T14N (p.Thr14Asn) variant details
- p.Thr14Asn
- TOPMed rs1188604193
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available